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采用循环伏安法研究了碳纳米管修饰玻碳电极对抗坏血酸的电催化活性。研究表明,碳纳米管修饰玻碳电极对抗坏血酸具有优异的电催化活性,与裸玻碳电极相比,抗坏血酸在该修饰电极上的氧化峰电位负移0.502 V,氧化峰电流增加78%;抗坏血酸浓度在1.0×10-5~0.1 mol/L范围内呈良好线性关系,最低检测限为1.0×10-6 mol/L。 相似文献
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采用滴涂法将适量碳纳米管修饰到热解石墨电极上,后电沉积纳米氧化镍得到MWCNT/NiO/PG复合修饰电极。研究了它的电化学行为,并用于抗坏血酸的测定。试验表明,在pH=6的磷酸盐缓冲溶液中,抗坏血酸在修饰电极上产生一灵敏的氧化峰。当抗坏血酸的浓度在1.0×10-5~5.0×10-4 mol/L时,氧化峰电流与浓度呈线性关系,线性方程为:I(uA)=-0.4458-0.5922C(mmol/L),相关系数为R=-0.9989。检出限低至5.5×10-7 mol/L。该传感器重现性、稳定性、抗干扰性良好。 相似文献
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采用电聚合法制备了铁氰化铈纳米膜修饰玻碳电极,用扫描电镜(SEM)对修饰膜进行了表征。利用循环伏安(CV)法研究了对苯二酚(HQ)在该电极上的电化学行为。结果表明,与裸电极相比,HQ在铁氰化铈纳米膜修饰电极上的氧化峰峰电流有明显增高。用示差脉冲伏安(DPV)法在优化条件下检测出HQ在1.0×10-5~6.0×10-4mol/L浓度范围内与氧化峰电流有良好的线性关系,线性相关系数R=0.998。信噪比为3时,HQ的检出限为1.0×10-6mol/L。用该方法对环境水样中的HQ进行了分析,回收率为95.2%~104.8%。 相似文献
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《广东化工》2018,(19)
本文建立了基于计时电流法的碳纳米管修饰阵列电极同时检测抗坏血酸和尿酸的方法。首先制作了由两个碳工作电极(1mm×2mm)、一个大面积碳对极(2mm×13mm)和一个厚膜Ag/AgCl参比电极构成的集成化碳阵列电极系统,然后以多壁碳纳米管修饰碳阵列电极,最后分别在CH1道电极电位为0.211V测定了抗坏血酸,在CH2道电极电位为0.428V测定了尿酸。实验结果表明,通过聚乙烯不干胶掩膜模板和手工丝网印刷碳技术制作的阵列电极电极面积一致,电活性好。CH1道氧化峰电流(I_(pCH1))与抗坏血酸浓度在4.0×10~(-6) mol/L~4.0×10~(-5)mol/L呈良好的线性关系,CH2道氧化峰电流(I_(pCH2))尿酸浓度在4.0×10~(-7) mol/L~4.0×10~(-6) mol/L呈良好的线性关系。本文设计的电极和建立的测定方法在多种生物样品的同时测定方面具有潜在的价值。 相似文献
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《广州化工》2016,(12)
采用滴涂法在玻碳电极上修饰氧化石墨烯及多壁碳纳米管,通过电化学还原方法制备石墨烯/多壁碳纳米管复合材料及相应修饰电极(ERGO/MWCNTs/GCE)。运用循环伏安法研究多巴胺(DA)在修饰电极上的电化学行为。研究表明:与裸玻碳电极相比,多巴胺在修饰电极上氧化峰与还原峰电位差为70 m V,峰电流显著提高,表明该电极对多巴胺具有较好的催化氧化作用。高浓度抗坏血酸的存在不影响多巴胺的测定。在优化实验条件下,多巴胺在4.8×10~(-7)~1.1×10~(-5)mol/L和1.1×10~(-5)~2.93×10~(-4)mol/L范围内呈良好的线性关系,检出限为8.7×10~(-8)mol/L,RSD为4.3%。 相似文献
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《国际聚合物材料杂志》2012,61(11):809-820
Thin films of polyaniline (PANi) and PANi–Zinc oxide (ZnO) nanocomposites have been synthesized by a spin-coating technique. The ZnO powder of particle size 50–60 nm was synthesized by sol–gel technique and the polyaniline was synthesized by chemical oxidative polymerization of aniline. The nanocomposite films were characterized by X-ray diffraction (XRD), scanning electron microscopy (SEM), Fourier transform infrared (FTIR), UV–Vis spectroscopy, and four probe technique, and the results were compared with polyaniline films. 相似文献
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B.T. Raut M.A. Chougule Shashwati Sen R.C. Pawar C.S. Lee V.B. Patil 《Ceramics International》2012,38(5):3999-4007
Polyaniline–CdS nanocomposites have been synthesized by spin coating technique. The nanocrystalline CdS powder of particle size 40–50 nm was synthesized by sol–gel technique and the polyaniline was synthesized by chemical oxidative polymerization of aniline. The composite films were characterized by X-ray diffraction (XRD), field effect scanning electron microscopy (FESEM), Fourier transform infrared spectroscopy (FTIR), UV–Vis spectroscopy and Four probe method. The results were compared with corresponding data on pure polyaniline films. The intensity of diffraction peaks for PANi–CdS composites is lower than that for CdS. The conductivity measurement shows that molecular chain constitution of polyaniline is the most important carrier in polyaniline–CdS nano composite. The optical studies showed that variation in band gap of polyaniline (3.40 eV) to 2.54 eV CdS which is attributed to the interaction of CdS nanoparticles with PANi molecular chains. 相似文献
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Kyung Seok Kang Chan Hyuk Jee Taeyoon Kim Ildoo Chung 《Polymer-Plastics Technology and Engineering》2017,56(2):117-122
Relatively narrow molecular weight distribution polyaniline/poly(4-styrene sulfonate) were synthesized by aqueous chemical oxidation polymerization using a dialysis membrane as the key to controlling the diffusion speed of the initiator. The optical, electrochemical, and electrical properties of the resulting polyaniline/poly(4-styrene sulfonate) were estimated by ultraviolet–visible–near infrared spectroscopy, cyclic voltammetry, and four-point probe. Compared to a bulk polyaniline/poly(4-styrene sulfonate), the resulting polyaniline/poly(4-styrene sulfonate) showed relatively high crystallinity according to X-ray diffraction, and their polydispersity indices ranged from 1.6 to 2.0 as a function of the reaction time. The electrical conductivities of the resulting polyaniline/poly(4-styrene sulfonates) were also enhanced gradually with increasing reaction time. 相似文献
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In order to improve the mechanical performance and water resistance of water-borne conducting polyaniline film, conducting polyaniline/polyurethane-silica hybrid film was prepared in aqueous solution employing silanol-terminated polyurethane and methyltriethoxysilane as sol-gel precursors. The hybrid film showed surface resistivity of 108 Ω even though the conducting polyaniline loading was only 10 wt% (or 1.5 wt% of polyaniline), and the mechanical performance as well as water resistance was significantly improved, making it suitable for antistatic application. Therefore, a practical route to water-borne processing of conducting polyaniline is disclosed. 相似文献
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聚苯胺微乳液合成及其电致变色性 总被引:9,自引:0,他引:9
用 (NH4) 2 S2 O8为氧化剂 ,在功能质子酸 水 正丁醇三元体系中 ,用微乳液法合成了聚苯胺。以聚苯胺的电导率和电致变色性能为标准 ,讨论了引发剂、DBSA、反应温度和反应时间对聚苯胺性能的影响 ,并对影响聚苯胺 /聚乙烯醇复合膜的性能因素作了初步探讨。结果表明 :与用常规乳液法合成的聚苯胺相比 ,用微乳液法合成的聚苯胺与聚乙烯醇所成的膜 ,其电导率提高了 2个数量级 ,电致变色性能也更好。 相似文献
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研究了用十二烷基苯磺酸(DBSA)、磺基水杨酸(SSA)、对氨基苯磺酸(ABSA)和柠檬酸(CA)4种有机酸作掺杂剂制备掺杂态聚苯胺DBSA-PANI、SSA-PANI、ABSA-PANI、CA-PANI的工艺,并制备了样品。经FT-IR和SEM分析表明:4种酸均具有掺杂态聚苯胺的特征吸收峰,其中DBSA-PANI和SSA-PANI的掺杂峰更明显;而ABSA和CA掺杂后的聚苯胺为微纳米粒子结构。大尺寸的有机酸离子掺杂在聚苯胺的链间,可更有效地减弱分子间的相互作用使聚苯胺溶解性提高,导电性增加。样品导电性能最好的是磺基水杨酸掺杂的聚苯胺,电导率接近1 S/cm。 相似文献
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《国际聚合物材料杂志》2012,61(3):244-254
Thin films of polyaniline (PANi) and PANi: titanium oxide (TiO2) composites have been synthesized by sol–gel spin coating technique. The TiO2 powder of particle size 50–60 nm was synthesized by the sol–gel technique and the polyaniline was synthesized by the chemical oxidative polymerization of aniline. The composite films were characterized by X-ray diffraction (XRD), atomic force microscopy (AFM), scanning electron microscopy (SEM), Fourier transform infrared (FTIR) spectroscopy, UV-vis spectroscopy and the four-probe method. The results were compared with corresponding data on pure polyaniline films. The intensity of diffraction peaks for PANi:TiO2 composites is lower than that for TiO2. The characteristic FTIR peaks of pure PANi are observed to shift to a higher wavenumber in PANi:TiO2 composite, which is attributed to the interaction of TiO2 particles with PANi molecular chains. The resistivity measurement shows that the molecular chain constitution of polyaniline is the most important carrier in the polyaniline: nano-TiO2 composite. 相似文献
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The properties of an electrolyte for acid bright copper deposition have been investigated. The influence of polyaniline dispersion, polysafranine dye (levelling component), poly(alkylene oxide) (wetting agent) or dialkyl disulfides (brightener) and combinations of these additives on the quality of electrodeposited coatings were studied. The presence of polyaniline dispersions increased the levelling ability by 16% and at the same time the concentration of the other additives could be considerably reduced. The electrolyte containing polyaniline dispersion could also be efficiently used under production conditions. 相似文献
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Morphology transition of selenious acid doped polyaniline from nanoflakes to nanorods and nanospheres was explored by changing the selenious acid-aniline (dopant-monomer) mole ratio in the aniline polymerization. The transition of polyaniline nanospheres to nanorods occurred when the dopant-monomer mole ratio was between 1 and 0.5. The formation of polyaniline nanorods was dominant when the dopant-monomer mole ratio is 0.5. At mole ratio 0.5, nanorods were obtained with the diameter at around 150 nm. At mole ratio 1, both the nanorods and nanospheres were formed and formation of the nanosphere is favored when the mole ratio is more than 1. When the mole ratio was low (0.125-0.03), polyaniline showed flakes like morphology. The morphology transition was studied by scanning electron microscopy and the molecular structure was confirmed by X-ray diffraction, FTIR and UV-vis spectroscopy. A simple and practical route to synthesize polyaniline nanostructures was demonstrated using selenious acid as effective dopant. The mechanism governing the formation of the polyaniline nanostructures is discussed. 相似文献